Br J Dermatol. 1997 Jun;136(6):939-42.

Systemic involvement in scleredema of Buschke associated with IgG-kappa paraproteinaemia.

Basarab T, Burrows NP, Munn SE, Russell Jones R.

Source

Department of Dermatology, Ealing Hospital, Southall, Middlesex, UK.

Abstract

Scleredema is a rare primary cutaneous mucinosis. Systemic involvement is uncommon and histological confirmation is often lacking. We report a case of a 60-year-old man with scleredema and evidence of mucin deposition on biopsies from multiple extracutaneous sites. The bone marrow, nerve, hepatic and salivary gland involvement seen on histology in our patient has not, to our knowledge, been previously reported in this condition.

PMID:: 9217831; [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms, Substances

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Case Reports

MeSH Terms

Substances

Immunoglobulin G

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